期刊文献+

蟾蜍灵激活低分化鼻咽癌细胞氯通道 被引量:4

Bufalin activates chloride channels in poorly differentiated nasopharyngeal carcinoma cells
下载PDF
导出
摘要 目的:研究蟾蜍灵(bufalin)对低分化鼻咽癌(CNE-2Z)细胞氯通道的激活作用以及通道的特性。方法:采用全细胞膜片钳技术记录蟾蜍灵激活CNE-2Z细胞膜电流并分析其电流特征。结果:细胞外灌流1μmol/L的蟾蜍灵可诱发CNE-2Z细胞产生一个氯电流,该电流潜伏期较长,为(12.1±6.4)min,其翻转电位接近氯离子平衡电位。该电流具有较明显的外向优势,没有明显的时间依赖性失活和电压依赖性失活。氯通道阻断剂他莫昔芬(tamoxifen)可完全抑制该电流,细胞外灌流高渗液也可完全抑制该电流。结论:蟾蜍灵可以激活CNE-2Z细胞氯通道产生氯电流,与容积激活性氯电流相比,该电流的潜伏期较长,并且有更明显的外向优势。 AIM:To investigate the activation of chloride channels induced by bufalin and the properties of the channels in poorly differentiated nasopharyngeal carcinoma(CNE-2Z)cells.METHODS:The technique of whole-cell patch clamp was used to record the chloride currents and to analyze the characteristics of the currents in CNE-2Z cells. RESULTS:A chloride current was slowly activated by extracellular application of bufalin(1μmol/L).The activation of the current was slower than that of the volume-activated chloride current,with an activation latency of(12.1±6.4)min. The reversal potential of the current was close to the calculated Cl^-equilibrium potential(E_(Cl)=-0.9 mV).The chloride current was outward-rectified and did not show significant time-dependent or voltage-dependent inactivation.The chloride channel blocker tamoxifen completely inhibited the outward and inward currents.The current was also completely inhibited by extra-cellular application of 47%hypertonic solution.CONCLUSION:Bufalin activates chloride channels and induces a chloride current in CNE-2Z cells.Compared with the volume-activated chloride current in CNE-2Z cells,the activation latency of the bufalin-induced current is longer and the outward rectification is more obvious.
出处 《中国病理生理杂志》 CAS CSCD 北大核心 2011年第4期672-676,共5页 Chinese Journal of Pathophysiology
基金 国家自然科学基金资助项目(No.30771106 No.30870567 No.30871267 No.90913020 No.U0932004) 广东省自然科学基金资助项目(No.07005974) 广东医学院青年基金资助项目(No.XQ06013)
关键词 蟾蜍灵 鼻咽肿瘤 氯通道 Bufalin Nasopharyngeal neoplasms Chloride channels
  • 相关文献

参考文献10

二级参考文献35

  • 1金波,孙林,刘云鹏,卢香兰,田昕,梁再赋.蟾蜍毒素的部分分离纯化及其抗白血病作用[J].中国医科大学学报,2004,33(6):517-519. 被引量:16
  • 2孙雪荣,王立伟,毛建文,朱林燕,聂思槐,钟平,陈丽新.人胎儿鼻咽上皮细胞的背景氯电流[J].生理学报,2005,57(3):349-354. 被引量:13
  • 3Liu T,Brouha B,Grossman D,et al.Rapid induction of mitochondrial events and caspase-independent apoptosis in Survivin-targeted melanoma cells.Oncogene,2004,23:39-48.
  • 4Masuda Y,Kawazoe N,Nakajo S,et al.Bufalin induces apoptosis and influences the expression of apoptosis-related genes in human leukemia cells.Leuk Res,1995,19:549-556.
  • 5Watabe M,Kawazoe N,Masuda Y,et al.Bcl-2 protein inhibits bufalin-induced apoptosis through inhibition of mitogen-activated protein kinase activation in human leukemia U937 cells.Cancer Res,1997,57:3097-3100.
  • 6Raisova M,Hossini AM,Eberle J,et al.The Bax/Bcl-2 ratio determines the susceptibility of human melanoma cells to CD95/Fas-mediated apoptosis.J Invest Dermatol,2001,117:333-340.
  • 7Kawazoe N,Aiuchi T,Masuda Y,et al.Induction of apoptosis by bufalin in human tumor cells is associated with a change of intracellular concentration of Na + ions.J Biochem (Tokyo),1999,126:278-286.
  • 8Shin S,Sung BJ,Cho YS,et al.An anti-apoptosis protein human survivin is a direct inhibitor of caspase-3 and -7.Biochemistry,2001,40:1117-1123.
  • 9Song Z,Yao X,Wu M.Direct interaction between survivin and Smac/DIABLO is essential for the anti-apoptotic activity of survivin during taxol-induced apoptosis.J Biol Chem,2003,278:23130-23140.
  • 10Wang C, Chen T, Zhang N, et al. Melittin, a major component of bee venom, sensitizes human hepatocellular carcinoma cells to tumor necrosis factor - related apoptosis - inducing ligand (TRAIL) - induced apoptosis by activating CaMKII -TAK1 -JNK/p38 and inhibiting IkappaBalpha kinase - NFkappaB [ J]. J Biol Chem,2009, 284(6) :3804 -3813.

共引文献68

同被引文献37

  • 1李锋,马志方.蟾蜍灵对前列腺癌PC3细胞增殖和凋亡的作用及其机制[J].中华临床医师杂志(电子版),2011,5(22):6594-6598. 被引量:5
  • 2Liu J. Oleanolic acid and ursolic acid: research perspectives. J Ethnopharmacol 2005; 100(1-2): 92-94.
  • 3Dorai T, Aggarwal BB. Role of chemopreventive agents in cancer therapy. Cancer Lett 2004; 215(2): 129-140.
  • 4Novotny L, Vachalkova A, Biggs D. Ursolic acid: an antitumorigenic and chemopreventive activity. Minireview. Neoplasma 2001; 48(4): 241-246.
  • 5Lauthier F, Taillet L, Trouillas P, Delage C, Simon A. Ursolic acid triggers calcium-dependent apoptosis in human Daudi cells. Anticancer Drugs 2000; 11(9): 737-745.
  • 6Achiwa Y, Hasegawa K, Komiya T, Udagawa Y. Ursolic acid induces Bax-dependent apoptosis through the caspase-3 pathway in endometrial cancer SNG-Ⅱ cells. Oncol Rep 2005; 13(1): 51-57.
  • 7Kassi E, Sourlingas TG, Spiliotaki M, Papoutsi Z, Pratsinis H, Aligiannis N, Moutsatsou E Ursolic acid triggers apoptosis and Bcl-2 downregulation in MCF-7 breast cancer cells. Cancer Invest 2009; 27(7): 723-733.
  • 8Tang C, Lu YH, Xie JH, Wang F, Zou JN, Yang JS, Xing YY, Xi T. Downregulation of survivin and activation of caspase-3 through the PI3K/Akt pathway in ursolic acid-induced HepG2 cell apoptosis. Anticancer Drugs 2009; 20(4): 249- 258.
  • 9Li Y, Xing D, Chen Q, Chen WR. Enhancement of chemotherapeutic agent-induced apoptosis by inhibition of NF- kappaB using ursolic acid. Int J Cancer 2010; 127(2): 462 -473.
  • 10Ovesna Z, Vachalkova A, Horvathova K, Tothova D. Pentacyclic triterpenoic acids: new chemoprotective compounds. Minireview. Neoplasma 2004; 51 (5): 327-333.

引证文献4

二级引证文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部